Van Hamme Evelien, Dewerchin Hannah L, Cornelissen Els, Nauwynck Hans J
Laboratory of Virology, Faculty of Veterinary Medicine, Ghent University, 9820 Merelbeke, Belgium.
J Gen Virol. 2007 Sep;88(Pt 9):2527-2532. doi: 10.1099/vir.0.82991-0.
In this study, kinetics of attachment and internalization of feline infectious peritonitis virus (FIPV) serotype I strain Black and serotype II strain 79-1146 were determined in feline monocytes from two cats and in Crandell feline kidney (CrFK) cells. Attached FIPV I (Black) particles were observed on almost all monocytes. Within 1 h, 17 particles were bound per cell and, within 1 min, 89 % of the bound particles were internalized. For FIPV II (79-1146), attachment was observed on 66 and 95 % of all monocytes from the two cats. After 1 h, respectively five and 20 particles were bound per cell (all cells considered). Within 1 min, 60 % of the bound particles were internalized. Internalization in monocytes was efficient and proceeded via endocytosis. In CrFK cells, attachment and internalization were less efficient, especially for FIPV I (Black), so this cell line is not suitable for studying FIPV entry.
在本研究中,测定了I型猫传染性腹膜炎病毒(FIPV)毒株Black和II型毒株79 - 1146在两只猫的猫单核细胞以及Crandell猫肾(CrFK)细胞中的吸附和内化动力学。几乎在所有单核细胞上都观察到了吸附的FIPV I(Black)颗粒。1小时内,每个细胞结合17个颗粒,1分钟内,89%的结合颗粒被内化。对于FIPV II(79 - 1146),在两只猫的所有单核细胞中,分别有66%和95%观察到吸附。1小时后,每个细胞分别结合5个和20个颗粒(所有细胞均计算在内)。1分钟内,60%的结合颗粒被内化。单核细胞中的内化效率高,通过内吞作用进行。在CrFK细胞中,吸附和内化效率较低,尤其是对于FIPV I(Black),因此该细胞系不适合用于研究FIPV的进入。